阴极
掺杂剂
材料科学
氧气
氧化物
兴奋剂
固体氧化物燃料电池
分析化学(期刊)
氧气输送
扩散
无机化学
化学工程
化学
物理化学
冶金
电极
光电子学
热力学
阳极
有机化学
工程类
物理
色谱法
作者
Lele Wang,Shoufu Yu,Liling Zhang,Yueyuan Gu,Lei Bi
标识
DOI:10.1016/j.ijhydene.2023.09.118
摘要
Transition metal elements were employed to customize the standard Sr2Fe1.5Mo0.5O6 (SFM) material, with the goal of improving the performance of the SFM cathode in proton-conducting solid oxide fuel cells (H–SOFCs). Sr2FeMo0.5X0.5O6 (X = Ni, Co, Mn, Zn) materials were prepared, but it was discovered that only the dopants Ni and Co can form a pure phase, whereas the dopants Mn and Zn produced an obvious secondary phase. When comparing oxygen vacancies and oxygen diffusion kinetics, utilizing the Co-dopant exhibited clear advantages. The Co-doped SFM had a higher oxygen vacancy content and faster oxygen diffusion kinetics than both the standard and Ni-doped SFM cathodes. The energy barrier for the oxygen reduction reaction (ORR) at the Co-doped SFM cathode was 0.76 eV, which was much lower than that for the SFM and Ni-doped SFM, which were 5.52 and 2.28 eV, respectively. As a result, the Co-doped SFM's cathode reaction was greatly accelerated, resulting in a high fuel cell performance of 1306 mW cm−2 at 700 °C. This finding suggests that using the appropriate dopant can alleviate the low-performance problem of the traditional SFM cathode, resulting in a promising cathode option for H–SOFCs.
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